"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 220724	NM_181882.3(PRX):c.1216G>A (p.Ala406Thr)	PRX (A406T)	Single nucleotide variant (3 prime UTR variant +1 more)	Charcot-Marie-Tooth disease +3 more	GConflicting classifications of pathogenicity
Select item 138817	NM_181882.3(PRX):c.731C>T (p.Ala244Val)	PRX (A244V)	Single nucleotide variant (3 prime UTR variant +1 more)	Charcot-Marie-Tooth disease +4 more	GBenign/Likely benign